Transcriptome-wide profiling of N6-methyladenosine via a selective chemical labeling method

被引:10
|
作者
Xie, Yalun [1 ]
Han, Shaoqing [1 ]
Li, Qiming [2 ]
Fang, Zhentian [1 ]
Yang, Wei [1 ]
Wei, Qi [1 ]
Wang, Yafen [1 ]
Zhou, Yu [2 ]
Weng, Xiaocheng [1 ]
Zhou, Xiang [1 ]
机构
[1] Wuhan Univ, Coll Chem & Mol Sci, Key Lab Biomed Polymers, Minist Educ, Wuhan, Peoples R China
[2] Wuhan Univ, Coll Life Sci, Wuhan, Hubei, Peoples R China
关键词
SINGLE-NUCLEOTIDE-RESOLUTION; 2-PHOTON FLUORESCENT-PROBE; NITRIC-OXIDE; N-NITROSAMINES; NUCLEAR-RNA; METHYLATION; N6-METHYLADENOSINE; DNA; NITROSATION; RESIDUES;
D O I
10.1039/d2sc03181g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Studies of chemical modifications on RNA have ushered in the field of epitranscriptomics. N-6-Methyladenosine (m(6)A) is the most typical RNA modification and is indispensable for basic biological processes. This study presents a chemical pulldown method (m(6)A-ORL-Seq) for transcriptome-wide profiling of m(6)A. Moreover, chemical labeling results in a specific reverse transcription (RT) truncation signature. This study has identified four thousand high-confidence m(6)A sites at single-base resolution in the human transcriptome. Unlike previously reported methods based on m(6)A-antibody or m(6)A-sensitive enzymes, the antibody/enzyme-free chemical method provides a new perspective for single-base m(6)A detection at the transcriptome level.
引用
收藏
页码:12149 / 12157
页数:9
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